美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA204963"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
50742-115-01 50742-115 HUMAN PRESCRIPTION DRUG DESIPRAMINE HYDROCHLORIDE desipramine hydrochloride TABLET ORAL 20180919 N/A ANDA ANDA204963 Ingenus Pharmaceuticals, LLC DESIPRAMINE HYDROCHLORIDE 75 mg/1 100 TABLET in 1 BOTTLE (50742-115-01)
50742-114-01 50742-114 HUMAN PRESCRIPTION DRUG DESIPRAMINE HYDROCHLORIDE desipramine hydrochloride TABLET ORAL 20180919 N/A ANDA ANDA204963 Ingenus Pharmaceuticals, LLC DESIPRAMINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (50742-114-01)
72189-391-30 72189-391 HUMAN PRESCRIPTION DRUG Desipramine HCL Desipramine HCL TABLET ORAL 20221116 N/A ANDA ANDA204963 Direct_Rx DESIPRAMINE HYDROCHLORIDE 10 mg/1 30 TABLET in 1 BOTTLE (72189-391-30)
50742-113-01 50742-113 HUMAN PRESCRIPTION DRUG DESIPRAMINE HYDROCHLORIDE desipramine hydrochloride TABLET ORAL 20180919 N/A ANDA ANDA204963 Ingenus Pharmaceuticals, LLC DESIPRAMINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (50742-113-01)
50742-117-50 50742-117 HUMAN PRESCRIPTION DRUG DESIPRAMINE HYDROCHLORIDE desipramine hydrochloride TABLET ORAL 20180919 N/A ANDA ANDA204963 Ingenus Pharmaceuticals, LLC DESIPRAMINE HYDROCHLORIDE 150 mg/1 50 TABLET in 1 BOTTLE (50742-117-50)
50742-112-01 50742-112 HUMAN PRESCRIPTION DRUG DESIPRAMINE HYDROCHLORIDE desipramine hydrochloride TABLET ORAL 20180919 N/A ANDA ANDA204963 Ingenus Pharmaceuticals, LLC DESIPRAMINE HYDROCHLORIDE 10 mg/1 100 TABLET in 1 BOTTLE (50742-112-01)
50742-116-01 50742-116 HUMAN PRESCRIPTION DRUG DESIPRAMINE HYDROCHLORIDE desipramine hydrochloride TABLET ORAL 20180919 N/A ANDA ANDA204963 Ingenus Pharmaceuticals, LLC DESIPRAMINE HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (50742-116-01)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase